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Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case
Parathyroid carcinomas are rare endocrine tumors which comprise 0.3-5.6% of all causes of hyperparathyroidism. 90% of them are hormonally active, while 10% of them may be non-functional. They mostly occur in a single parathyroid gland. Concurrent involvement of both parathyroid glands is quite rare....
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The African Field Epidemiology Network
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622813/ https://www.ncbi.nlm.nih.gov/pubmed/28979642 http://dx.doi.org/10.11604/pamj.2017.27.241.11503 |
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author | Dikmen, Kursat Bostanci, Hasan Gobut, Huseyin Yildiz, Alp Ertunc, Onur Celik, Ali Akin, Murat Taneri, Ferit |
author_facet | Dikmen, Kursat Bostanci, Hasan Gobut, Huseyin Yildiz, Alp Ertunc, Onur Celik, Ali Akin, Murat Taneri, Ferit |
author_sort | Dikmen, Kursat |
collection | PubMed |
description | Parathyroid carcinomas are rare endocrine tumors which comprise 0.3-5.6% of all causes of hyperparathyroidism. 90% of them are hormonally active, while 10% of them may be non-functional. They mostly occur in a single parathyroid gland. Concurrent involvement of both parathyroid glands is quite rare. A 57-year-old male patient was admitted to emergency department with the complaint of dyspnea. Thorax tomography revealed a retrosternal mass. The mass was thoracoscopically excised by thoracic surgeons. Histopathological examination result of the mass was reported as parathyroid carcinoma. Parathyroid scintigraphy performed and focal activity increase in the lower pole of the left lobe. Parathyroid hormone level was 118 pg/ml and calcium level was measured as 11.4 mg/dl. The patient with these findings was operated and pathological examination of excised left lower parathyroid tissue was reported as carcinoma. In addition, micropapillary carcinoma was detected in left thyroid lobectomy specimen.Our case was also unusual in that double parathyroid carcinoma, which is a rare condition, was hormonally inactive. We aimed to present our case in the light of the literature due to its rare occurrence. |
format | Online Article Text |
id | pubmed-5622813 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | The African Field Epidemiology Network |
record_format | MEDLINE/PubMed |
spelling | pubmed-56228132017-10-04 Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case Dikmen, Kursat Bostanci, Hasan Gobut, Huseyin Yildiz, Alp Ertunc, Onur Celik, Ali Akin, Murat Taneri, Ferit Pan Afr Med J Case Report Parathyroid carcinomas are rare endocrine tumors which comprise 0.3-5.6% of all causes of hyperparathyroidism. 90% of them are hormonally active, while 10% of them may be non-functional. They mostly occur in a single parathyroid gland. Concurrent involvement of both parathyroid glands is quite rare. A 57-year-old male patient was admitted to emergency department with the complaint of dyspnea. Thorax tomography revealed a retrosternal mass. The mass was thoracoscopically excised by thoracic surgeons. Histopathological examination result of the mass was reported as parathyroid carcinoma. Parathyroid scintigraphy performed and focal activity increase in the lower pole of the left lobe. Parathyroid hormone level was 118 pg/ml and calcium level was measured as 11.4 mg/dl. The patient with these findings was operated and pathological examination of excised left lower parathyroid tissue was reported as carcinoma. In addition, micropapillary carcinoma was detected in left thyroid lobectomy specimen.Our case was also unusual in that double parathyroid carcinoma, which is a rare condition, was hormonally inactive. We aimed to present our case in the light of the literature due to its rare occurrence. The African Field Epidemiology Network 2017-08-02 /pmc/articles/PMC5622813/ /pubmed/28979642 http://dx.doi.org/10.11604/pamj.2017.27.241.11503 Text en © Kursat Dikmen et al. http://creativecommons.org/licenses/by/2.0/ The Pan African Medical Journal - ISSN 1937-8688. This is an Open Access article distributed under the terms of the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Report Dikmen, Kursat Bostanci, Hasan Gobut, Huseyin Yildiz, Alp Ertunc, Onur Celik, Ali Akin, Murat Taneri, Ferit Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title | Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title_full | Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title_fullStr | Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title_full_unstemmed | Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title_short | Nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
title_sort | nonfunctional double parathyroid carcinoma with incidental thyroid micropapillary carcinoma: a rare case |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5622813/ https://www.ncbi.nlm.nih.gov/pubmed/28979642 http://dx.doi.org/10.11604/pamj.2017.27.241.11503 |
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